Variant report

Variant	rs933341
Chromosome Location	chr7:83743619-83743620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:83743073..83745524-chr7:83752305..83754687,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10261415	0.81[CHB][hapmap]
rs10279093	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10808306	0.81[CHB][hapmap]
rs12707615	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12707616	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12707617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1468344	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2067693	0.81[CHB][hapmap]
rs2372033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3801655	0.81[CHB][hapmap]
rs4732543	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4732545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6467987	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6467988	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs6964546	0.81[CHB][hapmap]
rs6974494	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6977306	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7781923	0.81[CHB][hapmap]
rs7783472	0.81[CHB][hapmap]
rs7785708	0.81[CHB][hapmap]
rs7793598	0.81[CHB][hapmap]
rs929334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs929335	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv888629	chr7:83722691-83896025	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1017884	chr7:83724138-83972995	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv538995	chr7:83724138-83972995	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83734400-83762800	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:83735600-83746600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:83736400-83744200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:83738200-83746800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:83739400-83744600	Enhancers	Fetal Heart	heart
6	chr7:83740000-83744600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:83740600-83744600	Enhancers	Fetal Lung	lung
8	chr7:83741200-83744000	Enhancers	Adipose Nuclei	Adipose
9	chr7:83741200-83744000	Enhancers	Colon Smooth Muscle	Colon
10	chr7:83741400-83753400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:83741800-83743800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr7:83741800-83744000	Enhancers	Rectal Smooth Muscle	rectum
13	chr7:83742000-83743800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:83742000-83744200	Enhancers	NH-A	brain
15	chr7:83742000-83745200	Enhancers	HUVEC	blood vessel
16	chr7:83742200-83743800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:83742200-83744000	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:83742200-83744000	Enhancers	Fetal Brain Female	brain
19	chr7:83742200-83744400	Enhancers	NHLF	lung
20	chr7:83742200-83745000	Enhancers	Fetal Stomach	stomach
21	chr7:83742400-83743800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:83742400-83744000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:83742400-83744000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:83742400-83744000	Enhancers	Brain Substantia Nigra	brain
25	chr7:83742400-83746000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:83742400-83746800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr7:83742800-83743800	Enhancers	Fetal Kidney	kidney
28	chr7:83742800-83744600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:83743000-83744600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:83743000-83745800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:83743000-83746000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:83743000-83746200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr7:83743000-83746800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:83743000-83747600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:83743000-83750400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:83743000-83756400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:83743200-83743800	Weak transcription	Brain Anterior Caudate	brain
38	chr7:83743200-83744000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:83743200-83751800	Weak transcription	NHDF-Ad	bronchial
40	chr7:83743200-83752600	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr7:83743400-83744000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr7:83743400-83746000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:83743400-83752400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:83743600-83743800	Flanking Active TSS	Fetal Brain Male	brain
45	chr7:83743600-83744000	Enhancers	Right Ventricle	heart
46	chr7:83743600-83744400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr7:83743600-83746600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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